Cycloadditions of Alkynes to Furans and Thiophenes: A Cobalt-Mediated

and Thiophenes: A Cobalt-Mediated "Enol Ether. Walk". Roland Boese,la Daniel F. Harvey,lb. Michael J. Malaska.lb and K. Peter C. Vollhardt*Jb. Departm...
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J. Am. Chem. SOC.1994,116, 11153-11154

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[2 2 2]Cycloadditions of Alkynes to Furans and Thiophenes: A Cobalt-Mediated "Enol Ether Walk"

11153

Scheme 1

Roland Boese,la Daniel F. Harvey,lb Michael J. Malaska.lb and K. Peter C. Vollhardt*Jb 2

Department of Chemistry, University of Califomia at Berkeley, and Chemical Sciences Division Lawrence Berkeley Laboratory Berkeley, Calfomia 94720 Institute for Inorganic Chemistry Universitat-GesamthochschuleEssen Universitatsstrasse 5-7, 45141 Essen, FRG Received August 5, 1994

Involvement of the 2,3-double bond of furan and thiophene in cycloadditions is relatively uncommon, usually limited to specific substrates or by special condition^.^^^^ Our finding that indoles,3a pyrroles,3b imidazoles? and uracils3d can be activated by CpCo to undergo cocyclizations with alkynes suggested an extension of these efforts to the title heterocycles, in particular because the latter constitute new brackets for the degree of aromaticity (furan lowest, thiophene h i g h e ~ t that ) ~ is subject to neutralization in these reactions and because the anticipated enol (thio)ether products exhibit potential synthetic utility? Of concern with respect to the outcome of the proposed scheme were literature reports that indicated that, while transition metal n-complexation to the heteroaromatics in question was feasible, such treatment could lead to a number of alternative further reactions, including C-H activation and ring opening.6 Indeed, cobalt-mediated [2 2 2lcycloaddition of l a to solvent3bis(trimethylsily1)acetylene (BTMSA, Scheme 1)7 gave not the expected 2a but rather the rearranged 3a in the form of sensitive hemiacetal 4a (47%,anomeric ratio 4:l), in which the spirofused enol ether bridge had migrated to furnish the lessstrained (MM2 calculations on the free ligands) propellane framework.

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(1) (a) Universitit-GH Essen. (b) University of California at Berkeley. (2) (a) Wagner-Jauregg, T. Synthesis 1980, 769-798. For recent examoles. see: (b) Rogers. C.: Keav. B. A. Svnletr 1991. 353-355. (c) Himbkrt, G.; Schlindwzn, H.-J.'; Maas, G. J. Ciem. Soc., Chem. Commun 1990. 405-406. -. . (3j (a? Grotjahn, D. B.; Vollhardt, K. P. C. J. Am. Chem. SOC. 1986, 108, 2091-2093. (b) Sheppard, G. S.; Vollhardt, K. P. C. J. Org. Chem. 1986, 51, 5496-5498. (c) Boese, R.; Knolker, H.-J.; Vollhardt, K. P. C. Angew. Chem., lnt. Ed. Engl. 1987, 26, 1035-1037. (d) Boese, R.; Rodriguez, J.; Vollhardt, K. P. C. Angew. Chem., Inf. Ed. Engl. 1991, 30, 993-994. (4)Gorelik, M. V. Russ. Chem. Rev. 1990, 59, 116-133. (5) See, for example: (a) Padwa, A.; Murphree, S. S. Org. Prep. Proc. lnt. 1991, 23, 545-568. (b) Lipshutz, B. H. Chem. Rev. 1986, 86, 795819. (c) Kinoshita, T.; Hirano, M.; Yoshida, N. Synthesis 1991,384-386. (d) Barluenga, J.; Tomis, M.; Suirez-Sobrino, A. Synletf 1990, 673-674. (e) Luh, T.-Y.; Ni, 2.4.Synthesis 1990, 89-103. (f) Frauenrath, H. Synthesis 1989,721-734. (6) (a) Sadimenko, A. P.; Gamovskii, A. D., Retta, N. Coord. Chem. Rev. 1993, 126, 237-318. For recent work, see: (b) Buys, I. E.; Field, L. D.; Hambley, T. W.; McQueen, A. E. D. J. Chem. Soc., Chem. Commun. 1994, 557-558. (c) Bianchini, C.; Meli, A,; Peruzzini, M.; Vizza, F.; Henera, V.; Shchez-Delgado, R. A. Organometallics 1994,13,721-730. (d) Jones, W. D.; Chin, R. M. J. Am. Chem. SOC.1994,116, 198-203. (e) Chen, H.; Hodges, L. M.; Liu, R.; Stevens, W. C., Jr.; Sabat, M.; Harman, W. D. J. Am. Chem. SOC.1994, 116, 5499-5500 and references therein. (7) All new compounds isolated exhibited satisfactory analytical and/or spectroscopic or (2d,3 0 X-ray data (see supplementary material). For the preparation of (or methods toward) starting materials, see: (a) Vereshchagin, L. I.; Kirillova, L. P.; Rechkina, A. V.; Kuimova, N. M. Zh. Org. Khim. 1971, 7, 907-912. (b) Corey, E. J.; Bock, M . G. Tetrahedron Left. 1975, 3269-3270. (c) Benneche, T.; Strande, P.; Undheim, K. Synthesis 1983, 762-763. (d) Carpenter, A. J.; Chadwick, D. J. Tetrahedron 1985, 41, 3803-3812. (e) Prugh, J. D.; Hartman, G. D.; Mallorga, P. J.; McKeever, B. M.; Michelson, S. R.; Murcko, M. A.; Schwam, H.; Smith, R. L.; Sondey, J. M.; Springer, J. P.; Sugrue, M. F. J. Med. Chem. 1991,34, 1805-1818. (f) Sick, J. J. Am. Chem. SOC. 1953, 75, 3697-3700. (9) Dowle, M. D.; Hayes, R.; Judd, D. B.; Williams, C. N. Synthesis 1983, 73-75.

l..X.S,R-nCo,Y.2.H I 1 X - S , R - C t b O , V - 2 - ti 71 X . S , R - 2 - H . Y - 0

Scheme 2" 4

m

L

E.

a (a) CuC12.2HzO) (4 equiv), CH3CN, 81%; (b) NaB& (4 equiv), (CH3)2CHOH, 79%;(c) CH3OH, HzS04,80%, or (CH&CHOH, H2S04, 84%, or C H ~ C O Z C O C H(CH3CH&N, ~, 91%; (d) NaB& (10 equiv), (CH3)zCHOH (1H NMR characterization); (e) SiOz, 80% from 4a; (f) CuC12 (5 equiv), CHsCN, 57%;(g) BF~.(CH~CHZ)~O (6 equiv), CH2C12,

83%.

Scheme 3

bA-O,B-CH w *.s,B.cn 1c *.CH,B.S

Proof of the structure of 4a was established by the extensive derivatization and correlation chemistry outlined in Scheme 2', including an X-ray It is of mechanistic relevance (vide infra) that 6a transforms predominantly by seeming C2-H activationlo to 7a (33%) and, remarkably, also (vide infra) to 4a (4%) as the sole products (Scheme 3): More telling is a labeling experiment with lb, providing 4b with deuterium extensively scrambled over positions a and b [Da:Db = 2: 1 (35 "C), 3.5:1 (90 "C); final ratios unchanged at 110 "C, 24 h]." Although Da:Db varies somewhat with the temperature of the cyclization, it remains unchanged in the product (110 "C,24 h)." A mechanism accommodating these results is shown in Scheme 4. It presupposes that the [2 2 2lcycloaddition proceeds initially as expected to generate 2 but that this species is capable of heterolytic ring-opening to the zwitterion A, featuring an enolate substituent attached to a relatively stable

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~

(8) Dessouki, R. S.; Hugi, A. D.; Wilisch, W. C. A. Acta Crystallogr., Sect. C 1987,43, 2340-2343. (9)Similar results were obtained with 1 (X = 0, R = CH3), 2-(4pentynyl)furan, and with l a and dimethyl butynedioate. (10) For analogies, see: (a) Yamazaki, H.; Wakatsuki, Y. J. Organomet. Chem. 1978,149, 377-393. (b) Selnau, H. E.; Merola, J. S. Organometallics 1993, 12, 3800-3801. (c) Robertson, M. J.; White, C. J.; Angelici, R. J. J. Am. Chem. SOC. 1994, 116, 5190-5195. (11) The position of the label was detected by 'H NMR experiments, most conveniently on 5, in which assignments were readily made by NOE experiments.

0002-7863/94/1516-11153$04.50/00 1994 American Chemical Society

Communications to the Editor

11154 J. Am. Chem. Soc., Vol. 116, No. 24, 1994

Scheme 4

ti

bz

6

&

--

"&A] SllCY I,

SllCHdi

St(CH&

L$pJ$T

1

7

\ & y W -w

9 ' SlIcHd, 3

3

CpCo cyclohexadienyl cation.lZ Collapse of A by C-C bond formation would produce norcaradienecarbaldehyde B, which could reopen to zwitterion C. The latter can furnish 3 (Z, = D) by direct closure at oxygen (kl) or traverse (kz) through another but now symmetrical norcaradienecarbaldehyde isomer D to E and then 3' ( z b = D and kl t k2). The metamorphosis of 2 to 3 (and 6a to 4a) may also be rationalized by formulating a combination of 1,3- (the 2,3-dihydrofuran-cyclopropanecarbaldehyde eq~ilibrium),'~ 3,5-,14and 1,5- (norcaradieneringwalk)15 sigmatropies, rendered less plausible by the insights gained with the thiophene analogs of la. Thus, IC underwent cycloaddition to BTMSA [5 equiv, toluene, 23 "C, CpCo (C2H&], providing 2c (8%) and 3c (25%). Likewise, Id leads to 2d only (43%), whereas l e and If gave 3e (3%) and 3f (37%), respectively, as the only isolable materials (Scheme 1). The structural assignments of the entire series are cemented by X-ray analyses of 2d and 3f.7 Surprisingly, IC and 3-hexyne converted to 7c (38%) exclusively, the result of formal C3-H activation, while 6b mimicked 6a (Scheme 3). The stereochemistry of the new diene unit in 7b,c was corroborated by NOE experiments. Mechanistically significant is that 2c, 2d, and 2e (prepared from 2d, 4-CH3C6hS03H, CH3COCH3, 23 "C, 58%) all underwent clean and essentially quantitative isomerization to 3c-e above 80 "C (C6H6 or toluene). Specifically, 2c followed first-order kinetics (C& or T w - d g ) with A@ = 27 & 1.5 kcal mol-' and A 9 = -7 rfr 4 cal K-l. The relative rates of conversion are in the order 2d:2c:2e = 1:2.7:5.5. More instructive is the effect of solvent polarity in the reorganization of 2c (95 "C): relative rates 1 (CaDIZ), 13 (c6D6), -16 (THFds), 258 (CD30D), >> 258 (CDFN), clearly consistent with rate(12) (a) Lai, Y.-H.; Tam, W.; Vollhardt, K. P. C. J. Organomet. Chem. 1981,216,97-103. (b) Stemberg, E. D.; Vollhardt, K. P. C. J. Org. Chem. 1984,49, 1564-1573. (c) Grotjahn, D. B.; Vollhardt, K.P. C. J. Am. Chem. SOC. 1990, 112, 5653-5654. (13) McGreer, D. E.; McKinley, J. W. Can. J. Chem. 1973, 51, 14871493 and references therein. (14) (a) Battye, P. J.; Jones, D. W.; Tucker, H. P. J. Chem. Soc., Chem. Commun. 1988, 495-496 and references therein. (b) Abramovitch, R. A.; Shinkai, I. J. Am. Chem. SOC. 1975, 97, 3227-3229. Zwitterions of the type A, C , and E on route to furopyridines are suggested. (15)(a) Baldwin, J. E.; B r o k e , B. M. J. Am. Chem. Soc. 1982, 104, 2857-2865 and references therein. (b) Brown, P. J. N.; Cadogan, J. I. G.; Gosney, I.; Johnstone, A. J. Chem. Soc., Chem. Commun. 1981, 10351036. A zwitterion of the type A, C, and E is suggested as an intermediate in the thermolysis of a norcaradienylketone.

determining formation of zwitterions of the type A (Scheme 4).16 A labeling experiment complementary to that using l b employed lg, cyclization of which produced 2g and 3g [Db:D, = 1.4:l (23 "C)]. Independent isomerization of 2g ('80 "C) ended in 3g with Db:D, = 2.7: 1 (unchanged by Si02 or heating to 130 "C for 56 h). Attempts to trap postulated intermediates A-E in the thermolysis of 2c with hydride,17 dienes,'* and e l e c t r ~ p h i l e shad ~ ~ no effect on the emergence of 3c. Oxidative demetalation (CuCly2H20, Et3N, CH3CN, 23 "C) of 2c-e required added Et3N to avoid decomposition and liberated the intact ligands 8 (-50%), which decomposed on heating (C6D6, 85 "C) or attempted recomplexation [C6D6, CpCo(CzH&]. On the other hand, propellane complex 3c released its ligand 9c (63%) unchanged only in the absence of Et3N, whereas the presence of the latter allowed isolation of the new isomer 10 (41%),lZcin addition to 9c (21%). Both isomers are stable at 80 "C (13 h) and to the oxidative demetalation mixture; 9c is also inert to exposure to CpCo(C2H4)2 (3 days, 23 "C). In contrast, 10 is reconstituted rapidly to the more stable 9c [MM2: AH"A9c) = 27.81 kcal mol-', W t ( l 0 c ) = 30.57 kcal with catalytic CpCo(C2H& (0.2 equiv, 15 min, 65%), presumably via a direct 1,5-shift mechanism perhaps mediated by a sulfur-complexedmetal. Be that as it may, it is clear that the enol ether "walk" (Scheme 4) requires the presence of the q4-diene CpCo unit. Finally, attempted decomplexation of 3f (no Et3N) effected chlorinationz0 to complex 11 (34%), while hydrolysis unmasked ketone 12 (4-CH3C&S03H, CH3COCH3, 23 "C, 21%). SIlCH?b

UI SlICHd, 10

11

12

In summary, this study demonstrates that the cobalt-mediated [2 2 21 methodology can be extended to furans and thiophenes but that in these, and possibly generally in related heteroalkenes, the generation of potential dienylic leaving groups in the resulting CpCo diene product may cause rearrangements and that formal C-H activations may complicate the outcome of the reaction. The observation that the relatively highly aromatic thiophene nucleus functions as a cocyclization partner points the way to a number of even more challenging substrates in this process.

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Acknowledgment. This study was supported by NIH Grant GM22479. D.F.H. was a Research Fellow of the Miller Institute for Basic Research in Science. Supplementary Material Available: Experimental, spectral, analytical, and X-ray (for 2d, 3 0 data for all new compounds (55 pages); observed and calculated structure factors for 2d and 3f (37 pages). This material is contained in many libraries on microfiche, immediately follows this article in the microfilm version of the journal, and can be ordered from the ACS; see any current masthead page for ordering information. (16) Reichardt, C. Solvents and Solvent Effects in Organic Chemistry; VCH: Weinheim, 1988. (17) Baldwin, J. E.; Jung, M. J. Chem. Soc., Chem. Commun. 1978,609610. (18) Bryce, M. R.; Becher, J.; Fat-Hansen, B. Adv. Heterocycl. Chem. 1992, 55, 1-29. (19) (a) Metzner, P.; Rakotonirina, R. Tetrahedron 1985, 41, 12891298. (b) Guignt, A.; Metzner, P. Phosphorus Sulfur 1985, 25, 97-102. (20)Kodomari, M.; Takahashi, S.; Yoshitomi, S. Chem. Lett. 1987, 1901- 1902.